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Journal Abstract Search
324 related items for PubMed ID: 9255907
1. Homozygous type I plasminogen deficiency. Mingers AM, Heimburger N, Zeitler P, Kreth HW, Schuster V. Semin Thromb Hemost; 1997; 23(3):259-69. PubMed ID: 9255907 [Abstract] [Full Text] [Related]
2. Polymorphonuclear elastase in patients with homozygous type I plasminogen deficiency and ligneous conjunctivitis. Mingers AM, Philapitsch A, Schwarz HP, Zeitler P, Kreth HW. Semin Thromb Hemost; 1998; 24(6):605-12. PubMed ID: 10066157 [Abstract] [Full Text] [Related]
3. Human homozygous type I plasminogen deficiency and ligneous conjunctivitis. Mingers AM, Philapitsch A, Zeitler P, Schuster V, Schwarz HP, Kreth HW. APMIS; 1999 Jan; 107(1):62-72. PubMed ID: 10190281 [Abstract] [Full Text] [Related]
6. Reduction of contact activation related fibrinolytic activity in factor XII deficient patients. Further evidence for the role of the contact system in fibrinolysis in vivo. Levi M, Hack CE, de Boer JP, Brandjes DP, Büller HR, ten Cate JW. J Clin Invest; 1991 Oct; 88(4):1155-60. PubMed ID: 1833421 [Abstract] [Full Text] [Related]
9. Intravascular and peritoneal coagulation and fibrinolysis in horses with acute gastrointestinal tract diseases. Collatos C, Barton MH, Prasse KW, Moore JN. J Am Vet Med Assoc; 1995 Aug 15; 207(4):465-70. PubMed ID: 7591947 [Abstract] [Full Text] [Related]
10. Fibrinolytic studies in 13 unrelated families with factor XII deficiency. Rodeghiero F, Castaman G, Ruggeri M, Cazzavillan M, Ferracin G, Dini E. Haematologica; 1991 Aug 15; 76(1):28-32. PubMed ID: 2055558 [Abstract] [Full Text] [Related]
11. [Studies of coagulation-fibrinolysis system and cold insoluble globulin in cases of caesarean section]. Mutoh S, Teh A, Shimoji Y, Nishi N, Saitoh M, Maki M. Nihon Sanka Fujinka Gakkai Zasshi; 1985 Oct 15; 37(10):2049-58. PubMed ID: 3878385 [Abstract] [Full Text] [Related]
14. The study of local fibrinolysis in abortion. Ikeuchi M. Nihon Sanka Fujinka Gakkai Zasshi; 1985 Jul 15; 37(7):1215-23. PubMed ID: 2411832 [Abstract] [Full Text] [Related]
18. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis]. Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M. Srp Arh Celok Lek; 1999 Dec 15; 127(1-2):21-7. PubMed ID: 10377836 [Abstract] [Full Text] [Related]